摘要
实时定量PCR(RT-q PCR)是确定基因功能的重要手段之一。为了量化基因表达水平,选择合适的内参基因是实验准确的先决条件。本文以小麦ACTIN1、ACTIN2、GAPDH、GAPDH2、ATUB、BTUB、EF1A1、EF1A2和TA共9个基因作为候选内参基因,在小麦(Triticum aesetrum)与叶锈菌(Puccinia triticina)互作过程中,利用RT-q PCR技术,检测这9个基因的表达情况。经ge Norm和Norm Finder软件分析可知,在小麦接种叶锈菌后不同时间点,GAPDH和TA基因的表达稳定性较高,可以作为RT-q PCR的内参基因。在此基础上,利用筛选得到的最适内参GAPDH对小麦与叶锈菌互作过程中,Ta SGR基因的相对表达量做了定量分析。结果显示,在亲和组合接种后中后期,Ta SGR基因的相对表达量迅速增加,达到了对照的近7倍水平,而在不亲和组合接种后不同时间点,Ta SGR基因的表达量与对照0 h相比差异均不明显。
Real time quantitative PCR （RT-qPCR） has many potential applications in the determination of gene function. The quality of reference gene plays an essential role in analyzing gene expression. In this study, we took nine genes widely used in wheat （Triticum aesetrum） as candidate reference genes and evaluated the ex- pression stability of the nine candidate genes, in the interaction between wheat and Puccinia triticina, by using RT-qPCR. With the help of geNorm and NormFinder, we analyzed the data of RT-qPCR and got the expression stability of the nine candidate genes. Our results showed that GAPDH and TA were most stable two genes which can be reliably used in the stress conditions assessed. Based on this, we took GAPDH as the reference gene and analyzed gene expression profiles of TaSGR in the interaction between wheat and Puccinia triticina. Our data showed that the relative expression of TaSGR had a rapid increase in the compatible combinations at middle and later time after inoculation, nearly seven times than the level of control. While in the incompatible combinations, the relative expression of TaSGR did not change obviously.
出处
《植物生理学报》
CAS
CSCD
北大核心
2015年第5期642-648,共7页
Plant Physiology Journal
基金
国家自然科学基金(31171472)
高等学校博士学科点专项科研基金(优先发展领域)(20111302130001)
河北省科技厅河北省应用基础研究计划重点基础研究项目(12967149D)
河北省人事厅留学人员科技活动项目(20120316)
